January 4th 2022
By Tony Hagen
Savings from adalimumab biosimilars, which won't enter the US market until 2023, account for a significant share of the total, investigators said.
January 3rd 2022
By Deana Ferreri, PhD
Patients with stage IV nonsquamous non–small cell lung cancer (NSCLC) demonstrated equivalent outcomes when treated with MYL-1402O or Avastin.
January 1st 2022
Biosimilars have produced more than $20 billion of savings in Europe, but more use of these agents is needed.
December 24th 2021
With fewer of the risks associated with novel drug development, biosimilar candidates allow manufacturers to plan far into the future for marketing needs.
December 23rd 2021
In Canada, a new jurisdiction inaugurates mandatory switching to biosimilars.
December 21st 2021
The year 2021 brought several firsts in biosimilars and set the stage for expansion across therapeutic areas including diabetes and ophthalmology.
December 20th 2021
A trio of regulatory experts discuss the current standing of biosimilar policy in the United States and expectations going forward.
Investigators said pathologic complete response (pCR) improved in a trastuzumab biosimilar/pertuzumab trial when patients were preselected for a subtype of breast cancer.
December 16th 2021
Investigators said more evidence would help to convince clinicians of the safety of switching between biosimilar products.
December 15th 2021
Xbrane Biopharma of Stockholm, Sweden, said its next biosimilar candidates will target the demand for oncology and hematology therapeutics.